Constructing Ru particles decorated Co3B-CoP heterostructures as a highly active and reusable catalyst for H2 generation by catalyzing NaBH4 hydrolysis

被引:32
|
作者
Zhou, Shuqing [1 ]
Cheng, Lianrui [1 ]
Huang, Yi [1 ]
Liu, Yi [1 ]
Shi, Luyan [1 ]
Isimjan, Tayirjan Taylor [2 ]
Yang, Xiulin [1 ]
机构
[1] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, Guangxi Key Lab Low Carbon Energy Mat, Guilin 541004, Peoples R China
[2] Saudi Arabia Basic Ind Corp SABIC, King Abdullah Univ Sci & Technol KAUST, Thuwal 239556900, Saudi Arabia
基金
中国国家自然科学基金;
关键词
Co3B-CoP; Electronic interaction; NaBH(4 )hydrolysis; Hydrogen generation; Catalytic mechanism; HYDROGEN GENERATION; RUTHENIUM(0) NANOCLUSTERS; COBALT NANOPARTICLES; SINGLE-ATOM; METAL; EVOLUTION; OXIDE; COP; FRAMEWORKS; CLUSTERS;
D O I
10.1016/j.apcatb.2023.122519
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Constructing an efficient and reusable catalyst for catalyzing NaBH4 hydrolysis for H-2 production is of vital significance. Herein, the Ru particles decorated Co3B-CoP heterostructures are obtained by chemical reduction and gas-phase phosphating treatment. The strong electronic interaction and abundant heterojunctions between the Co3B-CoP substrate and Ru particles have been elucidated. The optimal Ru-0.063/Co3B-CoP catalyst exhibits a fast hydrogen generation rate (8875.8 mL min(-1) g(cat)(- 1)) and a high turnover frequency (636.0 min(-1)) at 25 ?, superior to most ever reported catalysts. The excellent NaBH4 hydrolysis performance can be attributed to the lower activation energy (47.6 kJ mol(-1)) and the synergy between Co3B-CoP substrate and Ru particles. Density functional theory calculations show that electrons penetrate into Ru particles from Co3B-CoP substrate, in which the electron-rich Ru particles can selectively adsorb BH4- ions, while the electron-deficient Co3B-CoP facilitates the capture of H2O molecules, thereby synergistically promote the catalyzing NaBH4 hydrolysis to produce H-2.
引用
收藏
页数:9
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